
USFDA APPLICATION NUMBER - 20509 / DOSAGE - INJECTABLE;INJECTION - EQ 1GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
| Active Ingredient/Active Moiety | ||
| Ingredient Name | Basis of Strength | Strength |
|---|---|---|
| Gemcitabine hydrochloride(UNII: U347PV74IL) (Gemcitabine - UNII:B76N6SBZ8R) | Gemcitabine | 1g in 25 | 200mg in 5 |
Inactive Ingredients
| Ingredient Name | Eli Lilly and Company |
|---|---|
| Hydrochloric acid(QTT17582CB) | |
| Mannitol(3OWL53L36A) | |
| Sodium acetate(4550K0SC9B) | |
| Sodium hydroxide(55X04QC32I) |